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M L Budarf

Showing results (21-30 of 59) with videos related to

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Genomics|February 15, 1997
PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13G Matthijs, E Schollen, M Pirard, et al.
Genomics|April 1, 1989
Assignment of the human intestinal Na+/glucose cotransporter gene (SGLT1) to the q11.2----qter region of chromosome 22M A Hediger, M L Budarf, B S Emanuel, et al.
American Journal of Human Genetics|April 16, 1998
Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotypeS Gottlieb, D A Driscoll, H H Punnett, et al.
Immunogenetics|January 1, 1993
Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2T R Bauer, H E McDermid, M L Budarf, et al.
Genes, Chromosomes & Cancer|June 1, 1996
Narrowing the critical region for a rhabdoid tumor locus in 22q11J A Biegel, C S Allen, K Kawasaki, et al.
Human Molecular Genetics|June 22, 2000
Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, P Hu, et al.
American Journal of Human Genetics|May 1, 1997
The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human developmentS Gottlieb, B S Emanuel, D A Driscoll, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpointsK E McTaggart, M L Budarf, D A Driscoll, et al.
Human Molecular Genetics|February 1, 1997
Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical regionW Gong, B S Emanuel, N Galili, et al.
Genomics|August 1, 1997
Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 geneC Chieffo, N Garvey, W Gong, et al.
Pageof 6

Showing results (21-30 of 59) with videos related to

Sort By:
Pageof 6
Genomics|February 15, 1997
PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13G Matthijs, E Schollen, M Pirard, et al.
Genomics|April 1, 1989
Assignment of the human intestinal Na+/glucose cotransporter gene (SGLT1) to the q11.2----qter region of chromosome 22M A Hediger, M L Budarf, B S Emanuel, et al.
American Journal of Human Genetics|April 16, 1998
Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotypeS Gottlieb, D A Driscoll, H H Punnett, et al.
Immunogenetics|January 1, 1993
Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2T R Bauer, H E McDermid, M L Budarf, et al.
Genes, Chromosomes & Cancer|June 1, 1996
Narrowing the critical region for a rhabdoid tumor locus in 22q11J A Biegel, C S Allen, K Kawasaki, et al.
Human Molecular Genetics|June 22, 2000
Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22)H Kurahashi, T H Shaikh, P Hu, et al.
American Journal of Human Genetics|May 1, 1997
The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human developmentS Gottlieb, B S Emanuel, D A Driscoll, et al.
Cytogenetics and Cell Genetics|September 8, 1998
Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpointsK E McTaggart, M L Budarf, D A Driscoll, et al.
Human Molecular Genetics|February 1, 1997
Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical regionW Gong, B S Emanuel, N Galili, et al.
Genomics|August 1, 1997
Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 geneC Chieffo, N Garvey, W Gong, et al.
Pageof 6